{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83490",
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "address_1": "4100 E Milham Ave",
      "address_2": "N/A",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0024-2020",
      "product_description": "C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 07613327277319    Product Usage:  The C2 Nerve Monitor System is intended for intra-operative monitoring and stimulation for localization and identification of cranial and peripheral motor and mixed motor sensory nerves during surgery.",
      "product_quantity": "135",
      "reason_for_recall": "Stryker C2 NerveMonitor's design and instructions may not optimally address usability issues related to  the functionality of the device, which may result in use errors potentially causing or contributing to nerve  injury.",
      "recall_initiation_date": "20190731",
      "center_classification_date": "20191001",
      "termination_date": "20210324",
      "report_date": "20191009",
      "code_info": "All Serial Numbers are affected"
    }
  ]
}